反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 0 °C
PROCEDURE
实验过程
A solution of 3-bromoaniline (Aldrich; 1.3 equiv.) in methanol (0.4 M) was treated with 3-pyridinecarboxaldehyde (Aldrich; 1.0 equiv.). The solution was heated to reflux for 2 hours. The reaction was cooled to 0° C. and treated slowly with sodium borohydride (3.4 equiv.). After 1 hour the cooling bath was removed and stirring continued overnight. The reaction was concentrated in vacuo. The residue was partitioned between DCM and water. The aqueous phase was back-extracted once with DCM. The combined organics were washed with water and brine. The organic layer was concentrated to a white solid, which was purified via column chromatography eluting with 90:10 DCM/ethyl acetate to give N-(3-bromophenyl)pyridin-3-ylmethylamine. Anal Calcd for C12H11BrN2: C, 54.77; H, 4.21; N, 10.64. Found: C, 54.67; H, 4.19; N, 10.57. MS found 262.99, 264.99 [M+H]+
WORKUP
后处理
- temperatureThe solution was heated
- temperatureto reflux for 2 hours
- customAfter 1 hour the cooling bath was removed
- concentrationThe reaction was concentrated in vacuo
- customThe residue was partitioned between DCM and water
- extractionThe aqueous phase was back-extracted once with DCM
- washThe combined organics were washed with water and brine
- concentrationThe organic layer was concentrated to a white solid, which
- customwas purified via column chromatography
- washeluting with 90:10 DCM/ethyl acetate